Glioblastoma, Malignant Glioma
Conditions
Brief summary
This phase II trial studies how well fluorodopa F 18-positron emission tomography/magnetic resonance imaging scan (18F-DOPA-PET/MRI) works in imaging elderly patients with newly diagnosed grade IV malignant glioma or glioblastoma during planning for a short course of proton beam radiation therapy. 18F-DOPA is a chemical tracer that highlights certain cells during imaging. PET scan, is a metabolic imaging technique which takes advantage of how tumor cells take up nutrients differently than normal tissue. MRI scans are used to guide radiation therapy for most brain tumors. Hypofractionated proton beam therapy delivers higher doses of radiation therapy over a shorter period of time and may kill more tumor cells and have fewer side effects. Using 18FDOPA-PET scans along with MRI scans may be able to provide the radiation doctor with information on tumor tissue versus normal, healthy tissue and may help the doctor more accurately plan the radiation treatment.
Detailed description
PRIMARY OBJECTIVE: I. Compare overall survival at 12 months for grade IV glioma patients after radiation therapy targeting volumes designed with both 18F-DOPA-PET and conventional magnetic resonance (MR) image (or PET/computed tomography \[CT\]) information with historical controls. SECONDARY OBJECTIVES: I. Compare progression free survival at 12 months after radiation therapy targeting volumes designed with both 18F-DOPA-PET and conventional MR image information with historical controls. II. Determine acute and late effect toxicity after hypofractionated proton beam radiotherapy treatment including areas of high 18F-DOPA-PET uptake (T/N \> 2.0). CORRELATIVE RESEARCH OBJECTIVES: I. Compare radiotherapy (RT) treatment volumes defined by MR only with RT treatment volumes defined with both PET and MR information for grade IV glioma patients. II. Compare differences in RT volumes identified using biopsy-validated thresholds as highly aggressive disease comparing 18F-DOPA uptake and relative cerebral blood volume (relCBV) from perfusion MRI (pMRI) as well as differences in RT volumes identified using biopsy-validated thresholds as tumor extent comparing 18F-DOPA uptake and diffusion maps from diffusion tensor imaging (DTI) will be evaluated. III. Evaluate quality of life after radiotherapy using European Organization for Research and Treatment of Cancer (EORTC) questionnaires compared with historical controls from Keim-Guibert et al. IV. Compare differences in proton radiation planning utilizing radiobiologic modeling/evaluation techniques performed at Mayo Clinic Rochester to linear energy transfer distribution evaluation at Mayo Clinic Arizona. OUTLINE: Patients receive 18F-DOPA intravenously (IV) and undergo PET/MRI or PET/CT imaging scan. Patients then receive proton beam radiotherapy over 5 or 10 consecutive days excluding weekend and standard of care temozolomide on days 1-7 or 1-14. Beginning cycles 2, patients receive standard of care temozolomide on days 1-5. Cycles with temozolomide repeat every 28 days for up to 7 cycles in the in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 2 months for 1 year, and then periodically for up to 5 years.
Interventions
Ancillary studies
Ancillary studies
Drug
Undergo PET/CT
Given IV
Undergo PET/MRI
Undergo PET/CT or PET/MRI
Receive proton beam RT
Sponsors
Study design
Eligibility
Inclusion criteria
* Histologically confirmed newly diagnosed grade IV malignant glioma * Planned radiation treatments at Mayo Clinic Arizona or Mayo Clinic Rochester * Willing to sign release of information for any radiation and/or follow-up records * Provide informed written consent * Patients with estimated glomerular filtration rate (eGFR) \>= 60 mg/min/1.72 m\^2 * Ability to complete questionnaire(s) by themselves or with assistance * Eastern Cooperative Oncology Group (ECOG) performance status 0, 1, 2
Exclusion criteria
* Patients diagnosed with grades I-III glioma * Currently on Avastin at time of treatment * Unable to undergo MRI scans with contrast (e.g. cardiac pacemaker, defibrillator, kidney failure) * Unable to undergo an 18F-DOPA-PET scan (e.g. Parkinson's disease, taking anti-dopaminergic, or dopamine agonist medication or less than 6 half-lives from discontinuance of dopamine agonists) * NOTE: Other potentially interfering drugs: amoxapine, amphetamine, benztropine, buproprion, buspirone, cocaine, mazindol, methamphetamine, methylphenidate, norephedrine, phentermine, phenylpropanolamine, selegiline, paroxetine, citalopram, and sertraline. If a patient is on any of these drugs, list which ones on the on-study form * Pregnant women, nursing women, or men or women of childbearing potential who are unwilling to employ adequate contraception. * NOTE: All women enrolled in this study will be age 65 or over, and at the determination of the principal investigator (PI), will not be of childbearing potential. If the radiology department requires a pregnancy test before administering the 18FDOPA injection, they may perform one per their standard of care
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Overall Survival (OS) | Time from registration to death due to any cause, assessed up to 12 months | The proportion of successes will be estimated by the number of successes divided by the total number of evaluable patients. Confidence intervals for the true success proportion will be calculated utilizing exact binomial methodology. The distribution of survival time will be estimated using the method of Kaplan-Meier (1958). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Progression Free Survival | At 12 months after radiation therapy | Defined as the time from registration to the earliest date documenting disease progression |
| Incidence of Adverse Events (AEs) | Up to 4 years | The rate of acute and late treatment-related toxicities for newly diagnosed high-grade glioma patients treated with fluorodopa F 18-positron emission tomography (18F-DOPA PET) image-guided hypofractionated proton beam therapy will be determined, with acute radiotherapy (RT) toxicities graded using Common Terminology Criteria for Adverse Events (CTCAE) version 4.0. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Radiotherapy (RT) Treatment Volumes | Up to 5 years post treatment | Paired t-test statistical analysis will be performed to determine if any differences exist and the level of statistical significance between treatment volumes defined by magnetic resonance (MR) only and treatment volumes defined with both positron emission tomography (PET) and MR information. |
| Quality of Life (QOL) | Up to 5 years post treatment | QOL surveys will be compared to data from historical controls. Quality of life will be assessed at baseline and at each magnetic resonance imaging (MRI) evaluation (up to 6 evaluations). QOL will be measured using the European Organization for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30, a 30-item patient-reported questionnaire about patient ability to function, symptoms related to the cancer and its treatment, overall health and quality of life, and perceived financial impact of the cancer and its treatment. 28 of the 30 items are measured on a 1-4 scale (1=not at all; 4=very much) with the remaining two items (overall health and overall quality of life) scored on a 1-7 numeric analogue scale (1=very poor; 7=excellent). The recall period for the EORTC QLQ-C30 is one week. Higher scores indicate better QoL for overall health status and functioning scales, and worse QoL for symptom scales |
| Differences in Proton Radiation Planning | Up to 5 years post treatment | Paired t-test statistical analysis will be performed to determine if any differences exist and the level of statistical significance between proton plan metrics based off two modeling/evaluation techniques: radiobiologic modeling/evaluation techniques performed at Mayo Clinic Rochester and Linear Energy Transfer (LET) distribution evaluation at Mayo Clinic Arizona |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) Patients receive 18F-DOPA IV and undergo PET/MRI or PET/CT imaging scan. Patients then receive proton beam radiotherapy over 5 or 10 consecutive days excluding weekend and standard of care temozolomide on days 1-7 or 1-14. Beginning cycles 2, patients receive standard of care temozolomide on days 1-5. Cycles with temozolomide repeat every 28 days for up to 7 cycles in the in the absence of disease progression or unacceptable toxicity.\> \> Computed Tomography: Undergo PET/CT\>
\> Fluorodopa F 18: Given IV\>
\> Magnetic Resonance Imaging: Undergo PET/MRI\>
\> Positron Emission Tomography: Undergo PET/CT or PET/MRI\>
\> Proton Beam Radiation Therapy: Receive proton beam RT\>
\> Quality-of-Life Assessment: Ancillary studies\>
\> Questionnaire Administration: Ancillary studies\>
\> Temozolomide: Drug | 39 |
| Total | 39 |
Withdrawals & dropouts
| Period | Reason | FG000 |
|---|---|---|
| Overall Study | Death | 1 |
| Overall Study | disease progression before treatment | 2 |
| Overall Study | Issues with insurance | 1 |
Baseline characteristics
| Characteristic | Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) |
|---|---|
| Age, Continuous | 71.617 years STANDARD_DEVIATION 5.097 |
| Corticosteroid therapy at study entry? No | 18 Participants |
| Corticosteroid therapy at study entry? Yes | 21 Participants |
| ECOG Performance Status 0 | 13 Participants |
| ECOG Performance Status 1 | 19 Participants |
| ECOG Performance Status 2 | 7 Participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 38 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 1 Participants |
| Extent of surgery Biopsy | 15 Participants |
| Extent of surgery Gross total resection | 16 Participants |
| Extent of surgery Subtotal resection | 8 Participants |
| Family history of brain tumor No | 38 Participants |
| Family history of brain tumor Yes | 1 Participants |
| History of seizure No | 29 Participants |
| History of seizure Yes | 10 Participants |
| MGMT Methylated | 13 Participants |
| MGMT Not available | 2 Participants |
| MGMT Unmethylated | 24 Participants |
| Neurological Deficit No | 26 Participants |
| Neurological Deficit Yes | 13 Participants |
| Path result/Molecular factors IDH1 mutant | 0 Participants |
| Path result/Molecular factors IDH1 Wildtype | 39 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants |
| Race (NIH/OMB) Black or African American | 1 Participants |
| Race (NIH/OMB) More than one race | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 1 Participants |
| Race (NIH/OMB) White | 37 Participants |
| Sex: Female, Male Female | 11 Participants |
| Sex: Female, Male Male | 28 Participants |
| Use of alternating electrical therapy No | 39 Participants |
| Use of alternating electrical therapy Yes | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 32 / 39 |
| other Total, other adverse events | 39 / 39 |
| serious Total, serious adverse events | 0 / 39 |
Outcome results
Overall Survival (OS)
The proportion of successes will be estimated by the number of successes divided by the total number of evaluable patients. Confidence intervals for the true success proportion will be calculated utilizing exact binomial methodology. The distribution of survival time will be estimated using the method of Kaplan-Meier (1958).
Time frame: Time from registration to death due to any cause, assessed up to 12 months
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Overall Survival (OS) | 0.54 proportion of successes |
Incidence of Adverse Events (AEs)
The rate of acute and late treatment-related toxicities for newly diagnosed high-grade glioma patients treated with fluorodopa F 18-positron emission tomography (18F-DOPA PET) image-guided hypofractionated proton beam therapy will be determined, with acute radiotherapy (RT) toxicities graded using Common Terminology Criteria for Adverse Events (CTCAE) version 4.0.
Time frame: Up to 4 years
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Incidence of Adverse Events (AEs) | Grade 2 Post Baseline | 34 Participants |
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Incidence of Adverse Events (AEs) | Grade 3 Post Baseline | 18 Participants |
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Incidence of Adverse Events (AEs) | Grade 4 Post Baseline | 5 Participants |
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Incidence of Adverse Events (AEs) | Grade 2 Acute | 27 Participants |
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Incidence of Adverse Events (AEs) | Grade 3 Acute | 7 Participants |
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Incidence of Adverse Events (AEs) | Grade 4 Acute | 0 Participants |
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Incidence of Adverse Events (AEs) | Grade 2 Late | 24 Participants |
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Incidence of Adverse Events (AEs) | Grade 3 Late | 14 Participants |
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Incidence of Adverse Events (AEs) | Grade 4 Late | 5 Participants |
Progression Free Survival
Defined as the time from registration to the earliest date documenting disease progression
Time frame: Up to 4 years
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Progression Free Survival | 6.9 months |
Progression Free Survival
Defined as the time from registration to the earliest date documenting disease progression
Time frame: At 12 months after radiation therapy
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Treatment (18F-DOPA, PET/MRI, PET/CT, Temozolomide) | Progression Free Survival | 0.72 proportion of successes |
Differences in Proton Radiation Planning
Paired t-test statistical analysis will be performed to determine if any differences exist and the level of statistical significance between proton plan metrics based off two modeling/evaluation techniques: radiobiologic modeling/evaluation techniques performed at Mayo Clinic Rochester and Linear Energy Transfer (LET) distribution evaluation at Mayo Clinic Arizona
Time frame: Up to 5 years post treatment
Quality of Life (QOL)
QOL surveys will be compared to data from historical controls. Quality of life will be assessed at baseline and at each magnetic resonance imaging (MRI) evaluation (up to 6 evaluations). QOL will be measured using the European Organization for Research and Treatment of Cancer (EORTC) quality of life questionnaire (QLQ)-C30, a 30-item patient-reported questionnaire about patient ability to function, symptoms related to the cancer and its treatment, overall health and quality of life, and perceived financial impact of the cancer and its treatment. 28 of the 30 items are measured on a 1-4 scale (1=not at all; 4=very much) with the remaining two items (overall health and overall quality of life) scored on a 1-7 numeric analogue scale (1=very poor; 7=excellent). The recall period for the EORTC QLQ-C30 is one week. Higher scores indicate better QoL for overall health status and functioning scales, and worse QoL for symptom scales
Time frame: Up to 5 years post treatment
Radiotherapy (RT) Treatment Volumes
Paired t-test statistical analysis will be performed to determine if any differences exist and the level of statistical significance between treatment volumes defined by magnetic resonance (MR) only and treatment volumes defined with both positron emission tomography (PET) and MR information.
Time frame: Up to 5 years post treatment